Device recall
Z-1614-2012: Coseal Surgical Sealant. Coseal is an adjunctive surgical sealant.
FDA device recall · Class II · Baxter Healthcare Services L.P.
Key facts
| Recall number (Z-number) | Z-1614-2012 |
|---|---|
| Recall event | 59861 |
| Product | Coseal Surgical Sealant. Coseal is an adjunctive surgical sealant. |
| Product code | NBE |
| Recalling firm | Baxter Healthcare Services L.P. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2012 |
| PMA numbers | P030039 |
| FEI number | 3000121413 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database